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FDA 510(k)

PLOTTER FOR AS-500

K-Number: K853922 · 1985-11-14

Decision Date1985-11-14
Product CodeBZH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PLOTTER FOR AS-500 is the device name listed in this FDA 510(k) record. The listed applicant is Riko Medical & Scientific Instrument Corp.. It received FDA 510(k) clearance on 1985-11-14 under 510(k) number K853922. The device is classified under product code BZH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PLOTTER FOR AS-500?

PLOTTER FOR AS-500 is a medical device that received FDA 510(k) clearance on 1985-11-14. The listed applicant is Riko Medical & Scientific Instrument Corp.. The 510(k) number is K853922.

When did PLOTTER FOR AS-500 receive FDA 510(k) clearance?

PLOTTER FOR AS-500 received FDA 510(k) clearance on 1985-11-14, under 510(k) number K853922.

Who is the listed applicant for PLOTTER FOR AS-500?

The FDA 510(k) record lists Riko Medical & Scientific Instrument Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PLOTTER FOR AS-500?

The FDA product code for PLOTTER FOR AS-500 is BZH.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Riko Medical & Scientific Instrument Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: BZH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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